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OpenTrials
Completed

NCT Number: NCT01949181

Blood, Hair and Lung Concentrations of Metals and Metalloids in Patients With Lung Cancer or Chronic Obstructive Pulmonary Disease

Prospective research to study the relationship between concentrations of metals/metalloids in blood, hair and lung tissue with the occurence of lung cancer or chronic obstructive pulmonary disease.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hopital Foch, Suresnes, Île-de-France Region, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients of 18 to 75 years of age.
  • Patients admitted for lung resection (either cancerous or non-cancerous) or lung transplant

Exclusion criteria

  • Patients with mental or physical conditions that prevent them giving their agreement for the study

Treatment and study plan

Lung surgery

Procedure

Primary outcomes

  1. Metals/metalloids concentration

    Time frame: Blood, hair and lung tissue are sampled during lung surgery

Sponsors and collaborators

Lead sponsor

Hopital Foch

Other

Registry information

Official study title

Relationship Between Blood, Hair and Lung Metals/Metalloids Concentration (Cadmium, Iron, Copper, Nickel, Chrome, Arsenic, Vanadium, Beryllium, and Zinc) and Lung Cancer or Chronic Obstructive Pulmonary Disease.

Acronym: Métaux/Poumons

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Sep 24, 2013
Registry last updated
May 3, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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